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- ...h [[natural selection]] and other [[evolution]]ary processes acts. Without mutation, there are no new [[gene]]s, no new [[allele]]s and, eventually, no evoluti ...], where mutations occur up to 100 times more frequently than the normal [[mutation rate]]. A hotspot can be at an unusual base, e.g., 5-methylcytosine.13 KB (2,019 words) - 00:14, 11 November 2007
- 97 bytes (13 words) - 06:26, 23 May 2008
- 12 bytes (1 word) - 00:14, 11 November 2007
- #REDIRECT[[mutation]]21 bytes (2 words) - 20:01, 21 June 2007
- Auto-populated based on [[Special:WhatLinksHere/Mutation]]. Needs checking by a human.1 KB (167 words) - 18:44, 11 January 2010
Page text matches
- #REDIRECT [[Mutation]]22 bytes (2 words) - 19:42, 21 June 2007
- #REDIRECT[[mutation]]21 bytes (2 words) - 20:02, 21 June 2007
- #REDIRECT[[mutation]]21 bytes (2 words) - 20:01, 21 June 2007
- #REDIRECT[[mutation]]21 bytes (2 words) - 20:05, 21 June 2007
- ...ts; originally thought to be inheritable but possibly due to a spontaneous mutation163 bytes (21 words) - 17:29, 30 July 2010
- An [[X-linked]] [[recessive]] form of [[spinal muscular atrophy]] due to a mutation of the gene encoding the [[androgen receptor]].167 bytes (22 words) - 15:32, 23 February 2010
- ...F, Buser AS, Teo SS, Tiedt R, Passweg JR et al.| title=A gain-of-function mutation of JAK2 in myeloproliferative disorders. | journal=N Engl J Med | year= 2001 KB (190 words) - 20:53, 22 August 2010
- (AIS) Due to a mutation in the androgen receptor such that genetically male individuals (XY) do not321 bytes (52 words) - 13:18, 14 January 2009
- {{r|Mutation}}324 bytes (41 words) - 14:51, 17 March 2010
- {{r|gene mutation}}251 bytes (35 words) - 14:39, 13 December 2008
- {{r|Mutation}}175 bytes (21 words) - 20:29, 11 November 2007
- {{r|Mutation}}237 bytes (27 words) - 01:00, 9 February 2010
- ...of high potassium levels, sodium channels fail to activate properly. The mutation causes single [[amino acid]] changes in parts of the channel which importan2 KB (233 words) - 15:46, 14 February 2009
- ...s with [[DNA]]-damaging mutagens. Neither method is useful for producing a mutation in a specific [[genome|genomic]] location, nor are the techniques applicabl ...ntroduced in the 1980s to surmount these difficulties and allow specific [[mutation]]s to be induced in [[mammal]]ian cells. Even a mammalian [[somatic]] [[cel2 KB (346 words) - 00:44, 8 May 2008
- ...ntricles, known as the bundle of Kent. The inherited form can be caused by mutation of PRKAG2 gene encoding a gamma-2 regulatory subunit of AMP-activated prote482 bytes (77 words) - 11:57, 2 July 2009
- {{r|Mutation}}493 bytes (63 words) - 16:51, 11 January 2010
- {{r|Mutation}}478 bytes (61 words) - 17:20, 11 January 2010
- {{r|Mutation}}545 bytes (72 words) - 17:10, 11 January 2010
- {{r|Mutation}}522 bytes (69 words) - 20:49, 11 January 2010
- ...indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Rom702 bytes (91 words) - 01:33, 11 June 2010
- {{r|Space Quest V: The Next Mutation}}516 bytes (78 words) - 09:06, 7 April 2010
- {{r|Mutation}}836 bytes (104 words) - 06:18, 23 May 2010
- {{r|Mutation}}606 bytes (81 words) - 21:04, 11 January 2010
- {{r|Mutation}}715 bytes (95 words) - 17:20, 11 January 2010
- {{r|Mutation}}643 bytes (89 words) - 05:10, 9 June 2009
- {{r|Mutation}}728 bytes (86 words) - 21:08, 17 April 2011
- {{r|Mutation}}869 bytes (109 words) - 16:26, 11 January 2010
- {{r|Mutation}}791 bytes (103 words) - 07:44, 8 January 2010
- {{r|Mutation}}831 bytes (112 words) - 19:43, 11 January 2010
- {{r|Mutation}}855 bytes (110 words) - 21:04, 11 January 2010
- ...le = Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers886 bytes (120 words) - 11:57, 24 October 2010
- Some used "[[mutation]]" to refer to variations with low allele frequency. ...if a different polypeptide sequence is produced they are ''[[nonsynonymous mutation|nonsynonymous]]''.7 KB (957 words) - 10:47, 30 March 2010
- {{r|Mutation}}1,006 bytes (130 words) - 10:50, 11 January 2010
- ...le = Efficacy of Bilateral Prophylactic Mastectomy in BRCA1 and BRCA2 Gene Mutation Carriers965 bytes (129 words) - 22:06, 22 August 2010
- ...s'' is the inability to respond to vaopressin, (for instance if there is a mutation affecting the V2 vasopressin receptor) and cannot be treated in this way. ...hypothalamic diabetes insipidus is most commonly a consequence of a point mutation in the vasopressin gene, usually in the region coding for vasopressin-assoc4 KB (506 words) - 09:39, 24 July 2011
- ...//www.blackwellpublishing.com/ridley/classictexts/wright.asp "The roles of mutation, inbreeding, crossbreeding and selection in evolution"] ''Proc. 6th Int. Co1 KB (149 words) - 23:10, 15 February 2009
- ...ooks at how large scale changes may be caused by evolutionary mechanisms—[[mutation]], [[migration]], [[genetic drift]], and [[natural selection]].<ref>[http:/1 KB (169 words) - 06:31, 31 May 2009
- Auto-populated based on [[Special:WhatLinksHere/Mutation]]. Needs checking by a human.1 KB (167 words) - 18:44, 11 January 2010
- ...h [[natural selection]] and other [[evolution]]ary processes acts. Without mutation, there are no new [[gene]]s, no new [[allele]]s and, eventually, no evoluti ...], where mutations occur up to 100 times more frequently than the normal [[mutation rate]]. A hotspot can be at an unusual base, e.g., 5-methylcytosine.13 KB (2,019 words) - 00:14, 11 November 2007
- ...indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Rom ...siology involving the [[voltage-gated potassium channel]]. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).."<4 KB (593 words) - 10:17, 25 March 2011
- ...man}}</ref> and the formation of 5-HOU is the largest contributor for this mutation, because the base that was formally a cytosine base paired with guanine, is4 KB (593 words) - 13:27, 19 June 2008
- ...] to promote [[natriuresis]], and hence a deficiency of this peptide, or a mutation of the receptor results in salt-sensitive hypertension in mice.1 KB (168 words) - 04:18, 14 May 2023
- ...e quantitative estimates of viral titers, measurement of recombination and mutation rates, the statistical validation of radioactive decay measurements, and th2 KB (255 words) - 23:05, 24 February 2010
- {{r|Mutation}} {{r|Mutation}}5 KB (593 words) - 10:53, 12 May 2023
- ...a pore through which ions flow, carrying type A potassium current (IA). A mutation in the Sh gene reduces the conductance of charge across the neuron since th2 KB (245 words) - 09:23, 14 September 2013
- ...test for some lissencephaly variants, but only those with a known genetic mutation. ...ncy. There are also a number of genetic causes of lissencephaly, including mutation of the [[reelin]] gene (on [[chromosome 7]]),<ref>Hong SE, Shugart YY, Huan7 KB (972 words) - 21:31, 9 July 2011
- Examples include prothrombin gene G-->A20210 mutation.<ref name="pmid9669991">{{cite journal| author=Margaglione M, Brancaccio V, | [[Methylenetetrahydrofolate reductase]] mutation||colspan="2" align="center"|No association4 KB (517 words) - 15:32, 12 November 2010
- {{r|Mutation}}2 KB (265 words) - 10:53, 11 January 2010
- ...I. A punctual mutation was found in nucleotide 1367 of the rpoBgene. That mutation show strains of rifampin-resistant M.leprae in two of the three patients t3 KB (505 words) - 17:04, 18 August 2010
- ...erimental evolution studies, those with rapid [[generation time]]s, high [[mutation rate]]s, large [[population size]]s, and small sizes increase the feasibili ...epistasis, the effect of each mutation declines with increasing numbers of mutation. Understanding whether the majority of genetic interactions are synergistic10 KB (1,507 words) - 02:21, 8 May 2008